Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | HCID 136018531 | HCID 136018531 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 136395933 | HCID 136395933 | — |
Reaction Steps
A mixture of 2-[4-(chloromethyl)-phenyl]-5,6-dihydro-1,2,4-triazolo[4,3-c]-quinazolin-3-one (Compound 20) (150 mg, 0.48 mmol) and dimethylamine (1 ml, 40% in H2O) in THF was heated at 40° C. for 1.5 hours. The reaction was extracted with CH2Cl2 (3×50 ml) and the combined organic layers were dried over Na2SO4 and evaporated under reduced pressure. The residue was dissolved in ethyl acetate and saturated HCl/ethyl acetate solution was added to yield 2-[4-(N,N-dimethylaminomethyl)phenyl]-5,6-dihydro-1,2,4-triazolo-[4,3-c]quinazolin-3-one hydrochloride (Compound 21), m.p. 244-247° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05955465 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-69c18847668d497c8192207c78f631e8 |
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| Source note | uspto-grants-1999_09 |
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